Elevated expression of a subset of interferon inducible genes in primary bone marrow cells expressing p185 Bcr-Abl versus p210 Bcr-Abl by DNA microarray analysis

被引:4
作者
Advani, AS
Dressman, HK
Quiroz, M
Taylor, GA
Pendergast, AM
机构
[1] Duke Univ, Dept Pharmacol & Canc Biol, Med Ctr, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Div Hematol & Oncol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Genet, Durham, NC 27710 USA
[4] Duke Univ, Dept Med & Immunol, Div Geriatr, Durham, NC 27710 USA
[5] Duke Univ, Ctr Study Aging & Dev, Durham, NC 27710 USA
[6] VA Med Ctr, Durham, NC 27710 USA
关键词
Bcr-Abl; Philadelphia chromosome; chronic myelogenous leukemia; acute lymphocytic leukemia; interferon-gamma-inducible GTPases; microarray analysis;
D O I
10.1016/S0145-2126(03)00264-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
p185 Bcr-Abl has a more aggressive biological/clinical leukemia phenotype than p210 Bcr-Abl. In this study, we examined differential gene expression using microarrays to determine if Upregulation or downregulation of specific genes may explain the distinct phenotypes produced by the two Bcr-Abl forms. RNA was collected from mouse bone marrow mononuclear cells expressing equivalent levels of p 185 or p210, and the RNAs were subjected to microarray analysis. significant differences in gene expression were observed on hierarchical clustering. A group of interferon-gamma-inducible genes, including those encoding a family of 47 kDa GTPases, were significantly increased in p185 versus p210. This family of GTPases has previously been implicated in interferon-gamma-induced resistance against intracellular pathogens, however their exact cellular functions are unknown. Our data Suggest that their increased expression may contribute to the biological/clinical phenotype associated with p185. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:285 / 294
页数:10
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